New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32-Reference-Cited by-同舟云学术

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New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

Published:2013-06-01 Issue:6 Volume:70 Page:764
ISSN:2168-6149
Container-title:JAMA Neurology
language:en
Short-container-title:JAMA Neurol

Author:

Serrano-Munuera Carmen,Corral-Juan Marc,Stevanin Giovanni,San Nicolás Hector,Roig Carles,Corral Jordi,Campos Berta,de Jorge Laura,Morcillo-Suárez Carlos,Navarro Arcadi,Forlani Sylvie,Durr Alexandra,Kulisevsky Jaime,Brice Alexis,Sánchez Ivelisse,Volpini Victor,Matilla-Dueñas Antoni

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Supranuclear Vertical Gaze Palsy in Movement Disorders;Neuro-Ophthalmology;2024-07-17

2. A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex;Neuroscience Bulletin;2024-06-13

3. Novel genotype–phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC)n insertion in spinocerebellar ataxia type 37;Human Genetics;2024-02-23

4. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias;The Cerebellum;2023-03-31

5. Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18‐Year Study;Movement Disorders;2022-09-23

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